Laboratory Technician

Rangam Consultants Inc; North Carolina; On-site; USD 42,000 - 56,000; Full time

Job summary

Rangam Consultants seeks an organized sample coordination professional to support GMP pharma operations in a laboratory setting. The role entails managing daily sample activities, updating LIMS documentation, and training staff on procedures.

You will receive, inspect, and distribute samples, perform stability pulls, and maintain inventory and calendars for onsite and offsite storage, with potential for supervisory duties. A valid driver’s license and local travel are required.

Qualifications

• Three years of GMP pharma experience in a lab or sample management role.
• Ability to understand chemical hygiene and safety in a laboratory environment.
• Strong time management and organizational skills with consistent high-quality output.
• Strong verbal and written communication skills.
• Valid driver's license and vehicle for local travel.

Responsibilities

• Manage day-to-day activities of the sample coordination area and supervise at least one direct report.
• Maintain and update sample documentation in the LIMS system and train staff on its use.
• Receive and inspect incoming samples per Pearl procedures and governing documents.
• Pull samples, actuators, dose indicators, or related items and distribute to lab staff for testing; train staff.
• Perform stability sets and pulls per governing documents.
• Manage stability chamber inventory and calendar, notifying project staff of events.
• Pull and organize samples for shipment to Pearl sites or external groups.
• Prepare inventory lists periodically to aid disposal of unneeded samples.
• May back up daily chamber monitoring and chart recorder management.

Skills

GMP experience

Pharma lab

Sample management

Job description

Rangam Consultants is an award winning company for Staffing solutions and services. We are a multiple service provider in the Information Technology, Scientific, Engineering and administrative fields. We have a proven track record for successfully delivering mission critical consulting, support and recruiting services to various government and Fortune 500 clients.

Job Description

Manage the day-to-day activities of the sample coordination area and could have at least one direct report.

Responsibilities

• Maintain and update sample documentation in LIMS system and trains other sample coordination staff and analytical staff on use of system.
• Receive and inspect incoming samples and handle appropriately per Pearl procedures and governing documents
• Independently responsible for pulling samples, actuators, dose indicators, or any other sample configuration or related item and distribute to laboratory staff for testing. Trains other sample coordination staff on execution of these activities.
• Independently able to perform stability sets and pulls per Pearl governing documents
• Independently able to perform and document stability chamber inventory
• Maintains a stability pull calendar for onsite and offsite storage and proactively notifies project staff of upcoming events.
• Independently able to pull and organize samples for shipment to other Pearl sites or external groups
• Periodically prepare inventory list and distribute to laboratory management to facilitate disposal of samples that are no longer needed
• May serve as back up to daily chamber monitoring and chart recorder management and documentation

Requirements

• Three years of GMP pharma experience in a laboratory or sample management role with at least a year of sample management experience.
• Ability to understand and adhere to chemical hygiene and safety requirements while working in a laboratory environment.
• Must possess strong time management and organizational skills and an ability to adapt to a variety of tasks and execute them consistently to a high level of quality.
• Must possess strong communication verbal and written communication skills.
• Must be in possession of a valid driver's license and a vehicle suitable for local travel.

Physical Demands & Work Environment

Must be able to operate a PC. Some lifting required (not more than 50 lbs.). Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Additional Information

All your information will be kept confidential according to EEO guidelines.